Latest Managed Services Jobs

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Head of Data & BI Platform Engineering

Leads Pfizer's enterprise data and BI platform engineering, overseeing critical data infrastructure including data warehouses, ETL pipelines, and visualization tools. Responsible for platform strategy, reliability, governance, and enabling AI/ML workloads through scalable, secure data services. Works closely with federated analytics teams to ensure high availability, performance, and compliance across global data platforms.

Pfizer US$274,000 – US$456,600 pa

Hybrid Permanent

Head of Data & BI Platform Engineering

Leads Pfizer's enterprise data and BI platform engineering, overseeing critical data warehousing, integration, and visualization systems that underpin AI and analytics initiatives. Responsible for platform strategy, SLA-driven operations, and cross-functional collaboration to ensure reliable, governed access to data across the organization. Focuses on scaling cloud-based platforms like Snowflake and Databricks while aligning with AI-ready data standards and regulatory compliance.

Pfizer US$246,600 – US$411,000 pa

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards. You will act as a primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios and leading cross-functional discussions to resolve quality issues.

Novartis Ireland

Hybrid Permanent

Senior Scientific Engagement & Program Manager

This role involves planning and executing high-quality medical and scientific engagement activities across various therapeutic areas, including Oncology, Cardiovascular Disease, and Immunology. The Senior Scientific Engagement & Program Manager will coordinate advisory boards, congress activities, and medical education programs, ensuring seamless delivery and continuous improvement in processes and tools.

Novartis London, United Kingdom

Hybrid Permanent

Vice President, Head of Clinical Operations

This role involves leading the clinical operations strategy and execution across Recursion’s development portfolio, from study planning to study closeout. You will build and mentor a high-performing team, manage global trials, and ensure operational excellence in an AI-native TechBio company.

Recursion United Kingdom

On-site Permanent

DOCUMENT CONTROLLER

Compliance and Documentation AdministratorCrewe£28275 per annumFull-Time, PermanentAn excellent opportunity has arisen for an organised and detail-oriented Compliance and Documentation Adminitrator to join a successful and growing organisation operating within a highly regulated industry.This role is ideal for someone with strong...

KPI Recruiting Crewe Green, Cheshire, CW1 5UN, United Kingdom £28,275 pa

Associate Director, R&D Project Management

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...

CSL

Hybrid Permanent

Director, Portfolio Development Process & Standards Lead

This role leads the establishment and maintenance of processes and standards across CSL's global Portfolio Development function, ensuring high-quality clinical trial planning, evaluation, and reporting. The Director will drive process improvement, SOP governance, training curriculum development, and cross-functional change initiatives within a dynamic biotech R&D environment. They will work closely with leadership and international teams to reduce complexity, improve quality and speed, and align procedural frameworks across clinical development, biomarkers, and commercial operations.

CSL

Hybrid Permanent

R&D Scientist - Immunology

As an R&D Scientist, you will work in a state-of-the-art lab, generating high-quality immune profiling data using advanced cytometry and single-cell technologies. Your key responsibilities include performing flow cytometry assays, isolating immune cells from human blood, preparing samples for RNA sequencing, and maintaining quality control standards. You will collaborate with multidisciplinary teams and support ongoing research projects, with some weekend work required.

HAYS Specialist Recruitment London, United Kingdom £36,000 – £45,000 pa

On-site Permanent

Technical Program Coordinator, DDMR, London

As a Technical Program Coordinator, you will support the Drug Design and Medical Research (DDMR) function by managing program planning, monitoring timelines, tracking actions, and reporting risks. You will work closely with drug design teams, internal stakeholders, and external partners to ensure effective communication and alignment across the organization.

Isomorphic Labs London, United Kingdom

On-site Permanent

Director – Process Design and Optimisation in Chemical Development

This role involves leading a team in the design and optimisation of chemical processes for drug development. Responsibilities include technical direction, project delivery, regulatory submissions, and mentoring scientists. The position leverages innovative technologies and AI to enhance process efficiency and ensure robust commercial processes.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Head of Medicinal Chemistry, Drug Design, London

As Head of Medicinal Chemistry, you will lead a team of 25 chemists in London, driving the development of novel drugs using cutting-edge AI and machine learning. You will provide strategic direction, mentor team members, and collaborate with AI/ML scientists to accelerate drug discovery and clinical candidate nomination.

Isomorphic Labs London, United Kingdom

On-site Permanent

Medical Director, Patient Safety Physician

This role involves leading the clinical safety strategy for drug projects and products, evaluating safety data, and managing risk to patients. You will work closely with regulatory agencies, contribute to global submissions, and ensure the safety and efficacy of AstraZeneca's products throughout their lifecycle.

AstraZeneca Chatham, ME4 4NP, United Kingdom

Hybrid Permanent